Product code DPW— Cardiovascular

FloPatch FP120

Classification name
Flowmeter, Blood, Cardiovascular
Device class
Class 2
Regulation
21 CFR 870.2100
Advisory panel
Cardiovascular
Total cleared
138
First cleared
Most recent

Market context for product code DPW

FDA has cleared 138 devices under product code DPW between 1976 and 2026, filed by 85 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

Clearances per year

last 15 years

Top applicants under product code DPW

Recent clearances under product code DPW

1–100 of 138

Data sourced from openFDA. This site is unofficial and independent of the FDA.